% IMPORTANT: The following is UTF-8 encoded.  This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.

@ARTICLE{Kuttich:820727,
      author       = {Kuttich, B. and Ivanova, Oxana and Grillo, I. and Stühn,
                      B.},
      title        = {{P}olymer loaded microemulsions: {C}hangeover from finite
                      size effects to interfacial interactions},
      journal      = {The journal of chemical physics},
      volume       = {145},
      number       = {16},
      issn         = {1089-7690},
      address      = {Melville, NY},
      publisher    = {American Institute of Physics},
      reportid     = {FZJ-2016-05995},
      pages        = {164904 - 1-6},
      year         = {2016},
      abstract     = {Form fluctuations of microemulsion droplets are observed in
                      experiments using dielectric spectroscopy (DS) and neutron
                      spin echo spectroscopy (NSE). Previous work on dioctyl
                      sodium sulfosuccinate based water in oil microemulsions in
                      the droplet phase has shown that adding a water soluble
                      polymer (Polyethylene glycol M = 1500 g mol−1) modifies
                      these fluctuations. While for small droplet sizes (water
                      core radius rc < 37 Å) compared to the size of the polymer
                      both methods consistently showed a reduction in the bending
                      modulus of the surfactant shell as a result of polymer
                      addition, dielectric spectroscopy suggests the opposite
                      behaviour for large droplets. This observation is now
                      confirmed by NSE experiments on large droplets. Structural
                      changes due to polymer addition are qualitatively
                      independent of droplet size. Dynamical properties, however,
                      display a clear variation with the number of polymer chains
                      per droplet, leading to the observed changes in the bending
                      modulus. Furthermore, the contribution of structural and
                      dynamical properties on the changes in bending modulus
                      shifts in weight. With increasing droplet size, we initially
                      find dominating finite size effects and a changeover to a
                      system, where interactions between the confined polymer and
                      the surfactant shell dominate the bending modulus.I.
                      INTRODUCTION},
      cin          = {JCNS (München) ; Jülich Centre for Neutron Science JCNS
                      (München) ; JCNS-FRM-II / Neutronenstreuung ; JCNS-1},
      ddc          = {540},
      cid          = {I:(DE-Juel1)JCNS-FRM-II-20110218 /
                      I:(DE-Juel1)JCNS-1-20110106},
      pnm          = {6G15 - FRM II / MLZ (POF3-6G15) / 6G4 - Jülich Centre for
                      Neutron Research (JCNS) (POF3-623)},
      pid          = {G:(DE-HGF)POF3-6G15 / G:(DE-HGF)POF3-6G4},
      experiment   = {EXP:(DE-MLZ)J-NSE-20140101},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:000387586200050},
      doi          = {10.1063/1.4966155},
      url          = {https://juser.fz-juelich.de/record/820727},
}